Design of vaccine DNA containing genes encoding sicl Escherichia coli antigens Enterotoxigenic (ETEC) and Escherichia coli enterohemorrhagic (EHEC)

  • سال انتشار: 1399
  • محل انتشار: مجله تحقیقات پاتوبیولوژی، دوره: 23، شماره: 4
  • کد COI اختصاصی: JR_PRJMS-23-4_002
  • زبان مقاله: انگلیسی
  • تعداد مشاهده: 58
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نویسندگان

فاطمه جعفری پارسا

Department of Genetics, Faculty of Basic Sciences, Islamic Azad University, Research Sciences Branch, Tehran, Iran.

شهره زارع

Department of Genetics and Biotechnology, Pishva Faculty of Biological Sciences, Islamic Azad University, Varamin Branch, Iran.

سیدعلی میرحسینی

Applied Microbiology Research Center, Systems Biology and Poisonings Institute, Baqiyatallah University of Medical Sciences, Tehran- Iran.

جعفر امانی

Applied Microbiology Research Center, Systems Biology and Poisonings Institute, Baqiyatallah University of Medical Sciences, Vanak Sq. Molasadra St. Tehran- Iran.

چکیده

Introduction: Enterotoxigenic Escherichia coli (ETEC) and Enterohemorrhagic Escherichia coli O۱۵۷:H۷ , the most common strains,  are causes diarrhea that can kill  hundreds of thousands of children annually. The development of an effective combination vaccine for enterohemorrhagic Escherichia coli and Enterotoxigenic Escherichia coli is very important. Materials and Methods: In this study, the sicl gene was amplified and Subcloned as a DNA vaccine. The sequence of antigen encoding genes was evaluated from the genebank and their epitopes were evaluated to design of primer for the synthetic chimeric gene and was amplified by PCR. Subcloning of  a multipartal chimeric gene in eukaryotic expression vector was performed to make a DNA vaccine and finally the protein was purified by nickel chromatography and evaluated by Western blotting. Results: The immunoblotting results of the expression of SICL chimeric protein indicated the presence of a ۷۶ kDa band in the form of insoluble particles after ۱۲ hours induction. Purification of the recombinant protein using His tag sequencee and confirmation of the purified protein with the recombinant protein specific antibody demonstrated the accuracy of the protein expression. Discussion & Conclusion: Protein expression, purification and verify by western blotting showed that this recombinant chimeric protein (SICL) can be expressed in eukaryotic host.

کلیدواژه ها

Vaccine DNA, Enterotoxigenic Escherichia coli, Enterohemorrhagic Escherichia coli, Chimeric protein, DNA واکسن, اشریشیاکلی انتروتوکسیژنیک, اشریشیاکلی انتروهموراژیک, پروتئین کایمریک

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